Dipartimento di Scienze Biomediche, Università di Sassari, Viale S. Pietro 43/b, Sassari 07100, Italy.
Neurosci Biobehav Rev. 2024 Oct;165:105861. doi: 10.1016/j.neubiorev.2024.105861. Epub 2024 Aug 17.
Evidence on the effect of dopamine D1 and D2-like antagonists and of manipulations of reward value on licking microstructure is reanalysed considering recent findings on the role of nucleus accumbens (NAc) medium spiny neurons (MSNs) in the control of sugar intake. The results of this analysis suggest that D1 MSN activation, which is involved in the emission of licking bursts, might play a crucial role in response to novel rewards. D2 MSN activation, which results in reduction of burst size and suppression of licking, might mediate the response to reward devaluation. Elucidating the neural mechanisms underlying the licking response might lead to a better definition of its microstructural measures in behaviourally and psychologically meaningful functional terms. This could further support its use as a behavioural substrate in the study of the neural mechanisms of ingestive behaviour and motivation, as well as in animal models of pathological conditions such as eating disorders and obesity.
重新分析了多巴胺 D1 和 D2 样拮抗剂的作用以及操纵奖励价值对舔舐微观结构的影响的证据,同时考虑了最近关于伏隔核(NAc)中脑边缘系统神经元(MSNs)在控制糖摄入中的作用的发现。该分析的结果表明,参与舔舐爆发发射的 D1 MSN 激活可能在对新奖励的反应中起关键作用。D2 MSN 激活导致爆发大小减小和舔舐抑制,可能介导奖励贬值的反应。阐明舔舐反应的神经机制可能导致以行为和心理上有意义的功能术语更好地定义其微观结构测量。这可以进一步支持将其作为研究摄食行为和动机的神经机制以及饮食失调和肥胖等病理状况的动物模型中的行为底物的使用。